Package 0378-7292-53

{"route": ["ORAL"], "spl_id": "952f8023-4a5f-746d-c678-388b50e8909c", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961"], "spl_set_id": ["af851d82-b30f-463b-9dba-0437225dc1ee"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (0378-7292-53)  / 1 BLISTER PACK in 1 POUCH (0378-7292-85)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0378-7292-53", "marketing_start_date": "20130712"}], "brand_name": "NORETHINDRONE", "product_id": "0378-7292_952f8023-4a5f-746d-c678-388b50e8909c", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0378-7292", "generic_name": "norethindrone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA201483", "marketing_category": "ANDA", "marketing_start_date": "20130712", "listing_expiration_date": "20261231"}